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VALÉ: A Multidisciplinary Childhood Obesity Treatment Program for Latino Communities

Vidas Activas, famiLias saludablEs (Active Lives, Healthy Families) (VALÉ)

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04677582
Acronym
VALÉ
Enrollment
140
Registered
2020-12-21
Start date
2017-10-04
Completion date
2021-07-31
Last updated
2020-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pediatric Obesity

Brief summary

This proposal aims to test the initial feasibility and efficacy of a 10-week multidisciplinary pediatric weight management program among low-income Latino children, aged 5 to 11 years, from the Woodbridge, VA area. The following specific aims will be tested:

Detailed description

Specific Aim 1: To test the acceptability of a multidisciplinary group intervention targeted towards low-income Latino families with a child who is obese. Specific Aim 2: To test the effectiveness of the intervention by determining differences in behavioral changes (i.e. nutrition and physical activity habits), anthropometric (BMI-for-age, body fat) and clinical health outcomes (i.e. blood pressure, blood biomarkers) between children exposed to the intervention program vs. control children.

Interventions

BEHAVIORALVidas Activas, famiLias saludablEs (VALE)

Families and Children allocated to the intervention will receive weekly group-based meetings over a 10-week period consisting of education and activities on healthy lifestyles. Graduate students/Research Assistants trained in nutrition, exercise and clinical psychology will lead the meetings. All activities will be culturally relevant (i.e. cooking healthy Latino recipes) and Spanish speaking students will be recruited to deliver the intervention. Participants will be involved on deciding activities and projects and while some sessions will meet as a family group with parents/guardians, others will meet separately.

Sponsors

George Mason University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 11 Years
Healthy volunteers
Yes

Inclusion criteria

* Pre-pubertal (girls must not have started menses) * Of Latino/Hispanic descent (parent self-identified) * BMI for age \>85th percentile (based on CDC growth reference) * Child between 5-11 years old * Healthy (no known chronic diseases or regular medication) * Parent/adult caregivers willing to participate in all study visits

Exclusion criteria

* Not of Latino/Hispanic descent * \<5 years old or \>11 years old * BMI for age \<85th percentile * Not pre-pubertal (girls have experienced their first menses) * Child has learning deficits or acute/chronic medical condition * Parent/guardian has no transportation or unable to participate in sessions

Design outcomes

Primary

MeasureTime frameDescription
Change from Baseline BMI at 3 months and 6 monthsBaseline, 3 and 6 monthsbody weight (kg)/height(m\^2)
Change from Baseline Body Fat Percentage at 3 months and 6 monthsBaseline, 3 and 6 months% via bioelectric impedance
Change from Baseline Blood Pressure at 3 months and 6 monthsBaseline, 3 and 6 monthsSystolic & Diastolic Blood Pressure
Change from Baseline Waist Circumference at 3 months and 6 monthsBaseline, 3 and 6 monthscm
Change from Baseline HbA1c at 3 months and 6 monthsBaseline, 3 and 6 monthsHbA1c (%)
Change from Baseline Glucose at 3 months and 6 monthsBaseline, 3 and 6 monthsGlucose (mg/dL)
Change from Baseline Blood Lipids at 3 months and 6 monthsBaseline, 3 and 6 monthsLDL, HDL, TRG, TC (mg/dL)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026